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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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369 records meeting your search criteria returned- Product Code: KWL Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 42MM 11/26/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 7 11/16/2020
SMITH & NEPHEW ORTHOPAEDICS LTD UNKN BIRMINGHAM HIP RESURFACING (BHR) CU 11/10/2020
SMITH & NEPHEW ORTHOPAEDICS LTD MODULAR HEAD 42 MM +4 (LONG) 11/10/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 8 11/04/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 5 10/30/2020
DEPUY ORTHOPAEDICS INC US P.F.C.*NONPOROUS STEM #2 10/29/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 4 10/21/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 6 10/19/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 5 10/18/2020
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